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排序方式: 共有397条查询结果,搜索用时 12 毫秒
71.
James W. Goldfarb Agnes E. Holland Robert R. Edelman 《Magnetic resonance imaging》2001,19(10):I34-1274
The rest period of the coronary arteries has been shown to be on the order of 120–160 msec. Restriction of the acquisition window in breath-hold cardiac-synchronized gadolinium-enhanced imaging to this duration limits the amount of sampled k-space data and hence the information when compared with conventional gadolinium-enhanced imaging. Two techniques for gadolinium-enhanced cardiac-synchronized angiography were implemented that acquire additional data during the unused portions of the cardiac cycle. Data acquisition is synchronized with the heart cycle and is restricted to a short period of each heart cycle. In a single breath-hold, a multi-slab acquisition (n = 5) allowed ECG-synchronized imaging of the entire heart or a CINE acquisition (n = 5) provided multiple stacks of images at different phases in the cardiac cycle over a smaller area. Preliminary results acquired in healthy volunteers and patients with aortic disease indicate that additional information can be acquired without an increase in breath-hold duration or a reduction in image quality. 相似文献
72.
73.
Gary H. Posner Timothy P. Kogan Stephen R. Haines Leah L. Frye 《Tetrahedron letters》1984,25(25):2627-2630
A short, reliable, and practical synthesis of ()-(+)-2-(-tolylsulfinyl)-2-buten-4-olide has been developed, and the utility of this Michael acceptor for highly enantiocontrolled synthesis of 3-substituted 4-butanolides has been demonstrated. 相似文献
74.
Pinchas Aped Leah Schleifer Benzion Fuchs Saul Wolfe 《Journal of computational chemistry》1989,10(2):265-283
A study of systems containing the title moiety is described, with special reference to the anomeric effect. We have calculated ab initio, using Gaussian-80 with the 3-21G basis set, all basic conformations of methylene-diamine (H2N? CH2? NH2) and its N-methyl derivative with full geometry optimization of energy minima and barriers. The structural data thus obtained, were then employed to parameterize Allinger's MM2-80 force field in a procedure similar to that described for oxygen derivatives, including hydrogen-bonding effects and C? N bond shortening in tertiary amines. This modification, termed MM2-AE was then used to calculate larger molecules, including N,N′-di- and N,N,N′,N′-tetramethyl-methylenediamine, various 1,3-diazane systems, and 1,4,5,8-tetraazadecalin derivatives of established (x-ray) structures. The results are discussed in light of their verificative and predictive power and appear to validate MM2-AE as a useful computational procedure. 相似文献
75.
We study the implementation of two fundamentally different algorithms for solving the maximum flow problem: Dinic's method and the network simplex method. For the former, we present the design of a storage-efficient implementation. For the latter, we develop a "steepest-edge" pivot selection criterion that is easy to include in an existing network simplex implementation. We compare the computational efficiency of these two methods on a personal computer with a set of generated problems of up to 4 600 nodes and 27 000 arcs.This research was supported in part by the National Science Foundation under Grant Nos. MCS-8113503 and DMS-8512277. 相似文献
76.
Leah Susanne Mnkemller Martin Schnurr Bartosz Lewandowski 《Molecules (Basel, Switzerland)》2022,27(7)
Due to the chemical and biological relevance of amino acids, efficient methods for the recognition and separation of their enantiomers are highly sought after. Chiral receptors based on extended molecular scaffolds are typically employed for this purpose. These receptors are often effective only in specific environments and towards a narrow scope of amino acid guests. Recently we reported a simple, glucose-based macrocycle capable of enantioselective binding of a broad range of amino acid methyl esters in water. Herein we demonstrate that the same receptor can be used for chiral recognition of amino acid esters in organic solvents. We show that the binding affinity and selectivity of the receptor are highly dependent on the coordinating strength of the solvent. An in-depth analysis of the receptor’s conformation and its interactions with amino acid methyl esters allowed us to propose a binding mode of amino acids to the receptor in CDCl3. The binding modes in CDCl3 and D2O were then compared, highlighting the main interactions responsible for binding affinity and selectivity in each solvent. We envision that the insight provided by this study will facilitate the development of further amino acid receptors based on monosaccharides with improved binding affinities and both enantio- as well as chemoselectivities. 相似文献
77.
Dr. Esther Frederick Dr. Leah N. Appelhans Dr. Frank W. Del Rio Dr. Kevin T. Strong Jr. Dr. Sean Smith Sara Dickens Dr. Erika Vreeland 《Chemphyschem》2022,23(3):e202100673
Metal-organic framework (MOF) thin films currently lack the mechanical stability needed for electronic device applications. Polymer-based metal-organic frameworks (polyMOFs) have been suggested to provide mechanical advantages over MOFs, however, the mechanical properties of polyMOFs have not yet been characterized. In this work, we developed a method to synthesize continuous sub-5 μm polyUiO-66(Zr) films on Au substrates, which allowed us to undertake initial mechanical property investigations. Comparisons between polyUiO-66 and UiO-66 thin films determined polyUiO-66 thin films exhibit a lower modulus but similar hardness to UiO-66 thin films. The initial mechanical characterization indicates that further development is needed to leverage the mechanical property advantages of polyMOFs over MOFs. Additionally, the demonstration in this work of a continuous surface-supported polyUiO-66 thin film enables utilization of this emerging class of polyMOF materials in sensors and devices applications. 相似文献
78.
W-band (95 GHz) pulsed EPR and electron-nuclear double resonance (ENDOR) spectroscopic techniques were used to determine the hyperfine couplings of different protons of Cu(II)-histidine complexes in frozen solutions. The results were then used to obtain the coordination mode of the tridentate histidine molecule and to serve as a reference for Cu(II)-histidine complexation in other, more complex systems. Cu(II) complexes with L-histidine and DL-histidine-alpha-d,beta-d2 were prepared in H2O and in D2O, and orientation-selective W-band 1H and 2H pulsed ENDOR spectra of these complexes were recorded at 4.5 K. These measurements lead to the unambiguous assignment of the signals of the H alpha, H beta, imidazole H epsilon, and the exchangeable amino, Ham, protons. The 14N superhyperfine splitting observed in the X-band EPR spectrum and the presence of only one type of H alpha and H beta protons in the W-band ENDOR spectra show that the complex is a symmetric bis complex. Its g parallel is along the molecular symmetry axis, perpendicular to the equatorial plane that consists of four coordinated nitrogens in histamine-like coordinations (NNNN). Simulations of orientation-selective ENDOR spectra provided the principal components of the protons' hyperfine interaction and the orientation of their principal axes with respect to g parallel. From the anisotropic part of the hyperfine interaction of H alpha and H beta and applying the point-dipole approximation, a structural model was derived. An unexpectedly large isotropic hyperfine coupling, 10.9 MHz, was found for H alpha. In contrast, H alpha of the Cu(II)-1-methyl-histidine complex where only the amino nitrogen is coordinated, showed a much smaller coupling. Thus, the hyperfine coupling of H alpha can serve as a signature for a histamine coordination where both the amino and imino nitrogens of the same molecule bind to the Cu(II), forming a six-membered chelating ring. Unlike H alpha the hyperfine coupling of H epsilon is not as sensitive to the presence of a coordinated amino nitrogen of the same histidine molecule. 相似文献
79.
80.
Construction of an inexpensive surface plasmon resonance instrument for use in teaching and research
Barry K. Lavine David J. Westover Leah Oxenford Nikhil Mirjankar Necati Kaval 《Microchemical Journal》2007,86(2):147-155
The construction of an inexpensive SPR instrument that can be used for both teaching and research is described. Using a 2′ × 2′ optical table to construct this instrument allows both scientists and students full access to the operation of the spectrometer. Furthermore, the use of open platform instrumentation has the advantage of maintaining the focus on the relationship between emerging technology and analytical chemistry as well as allowing the user to modify the instrument to enhance the measurement process for a particular application. This is a change from the learning paradigm used in most research and teaching laboratories where commercial instrumentation is treated as a black box due to its complexity. Three studies, which were performed using this instrument, are presented to demonstrate the suitability of this instrument for both teaching and research. These studies include measuring the refractive index of alcohols, investigating the partitioning of ruthenium (II) trisbipyridine chloride into Nafion, and understanding the mechanism controlling metal ion adsorption by polyacrylamide hydrogels. 相似文献